OPTI-LENS(TM) CONTACT LENS CASE
K-Number: K915082 · 1992-01-13
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Device Summary
Frequently Asked Questions
What is the OPTI-LENS(TM) CONTACT LENS CASE?
OPTI-LENS(TM) CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1992-01-13. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K915082.
When did OPTI-LENS(TM) CONTACT LENS CASE receive FDA 510(k) clearance?
OPTI-LENS(TM) CONTACT LENS CASE received FDA 510(k) clearance on 1992-01-13, under 510(k) number K915082.
Who is the listed applicant for OPTI-LENS(TM) CONTACT LENS CASE?
The FDA 510(k) record lists Ryder Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTI-LENS(TM) CONTACT LENS CASE?
The FDA product code for OPTI-LENS(TM) CONTACT LENS CASE is LRX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Ryder Intl. Corp. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LRX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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